Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
NCT07558876

Task-Oriented Upper Limb Training With Focal Vibration in Stroke

Led by Jisu Kim · Updated on 2026-04-30

38

Participants Needed

2

Research Sites

40 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effects of task-oriented upper limb training combined with focal vibration on hand function, proprioception, and muscle tone in patients with stroke. Participants will be randomly assigned to either an experimental group receiving task-oriented training with concurrent focal vibration or a control group receiving task-oriented training alone. The intervention will be conducted over 6 weeks. Outcome measures will be assessed before and after the intervention.

CONDITIONS

Official Title

Task-Oriented Upper Limb Training With Focal Vibration in Stroke

Who Can Participate

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with stroke at least 3 months prior
  • Mini-Mental State Examination (MMSE) score of 24 or higher
  • Able to sit independently and perform upper limb functional tasks (Trunk Control Test score 50 or higher)
  • Muscle tone of affected upper limb Modified Ashworth Scale grade 2 or less
  • Fugl-Meyer Assessment-Upper Extremity scores between 20 and 50
  • Able to grasp and move objects with affected upper limb, Manual Muscle Test grade 3 or higher
  • Impaired proprioception in affected hand (score less than 2 on wrist or thumb position item of FMA-UE)
Not Eligible

You will not qualify if you...

  • Stroke onset less than 3 months ago
  • Fractures, severe soft tissue injuries, or contraindications to focal vibration
  • Severe sensory hypersensitivity or complex regional pain syndrome (CRPS)
  • Received treatments affecting upper limb function in past 3 months (e.g., botulinum toxin injection, surgery, nerve block)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Cheongdam Hospital

Seoul, South Korea

Actively Recruiting

2

Sahmyook University

Seoul, South Korea

Not Yet Recruiting

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Research Team

J

Jisu Kim, PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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